DOI QR코드

DOI QR Code

PM3 Studies on the Acid-Catalyzed Hydrolysis of 1-Phenoxyethyl Propionate

  • 발행 : 1998.09.20

초록

Acid catalyzed hydrolysis of 1-phenoxyethyl propionate, Ⅰ, has been studied using the PM3 method in the gas phase. The first step of the reaction is the protonation of basic sites, three different oxygens in Ⅰ, producing three protonated species Ⅱ, Ⅲ and Ⅳ. All possible reaction pathways have been studied from each protonated structure. Changes in the reaction mechanisms have also been discussed from the results obtained by varying a nucleophile from a water monomer to a water dimer to a complex between one water molecule and an intermediate product (propionic acid or phenol) produced in the preceding unimolecular dissociation processes. Minimum energy reaction pathway is 2-W among the possible pathways, in which water dimer acts as an active catalyst and therefore facilitates the formation of a six-membered cyclic transition state. Lower barrier of 2-W is ascribed to an efficient bifunctional catalytic effect of water molecules. PM3-SM3.1 single point calculations have been done at the gas-phase optimized structure (SM3.1/PM3//PM3) to compare theoretical results to those of experimental work.

키워드

참고문헌

  1. Chem. Rev v.69 Capon, B
  2. Adv. Phys. Org. Chem v.11 File, T. H
  3. J. Am. Chem. Soc v.87 File, T. H
  4. Advanced Organic Chemistry: reactions, mechanisms, and structure(4th ed.) March, J
  5. Can J. Chem v.53 McCelland, R. A
  6. J. Org. Chem v.51 Cox, R. A;Yates, J
  7. J. Chem. Soc. Perkin Trans v.2 Hall, C. D;Goulding, C. W
  8. J. Am. Chem. Soc v.101 Risley, J. M;Van Etten, R. L
  9. J. Am. Chem. Soc v.102 Vederas, J. C
  10. J. Am. Chem. Soc v.78 Bunton, C. A;Spatcher, D. P
  11. Acta Chem. Scand v.11 Salomaa, P
  12. Acta Chem. Scand v.17 Salomaa, P;Laiho, S
  13. Soumen Kemistilehti v.B37 Salomaa, P;Soumen Kemistilehti
  14. Acta Chem. Scand v.19 Salomaa, P;Sallinen, K. S
  15. J. Am. Chem. Soc v.91 Weeks, D. P;Zuorick, G. W
  16. J. Am. Chem. Soc v.90 Weeks, D. P;Grodski, A;Fauncci, R
  17. J. Org. Chem v.38 Weeks, D. P;Cella, J;Chen, L. T
  18. Mechanism and Structure in Organic Chemistry(2nd ed) Gould, E. S
  19. Physical Organic Chemistry, Longman Issacs, N. S
  20. Adv. Phys. Org. Chem v.5 Johnson,S. L
  21. J. Am. Chem. Soc v.86 Kirsch, j. F;Jencks, W. P
  22. J. Mol. Struc. (Theochem) v.208 Lee, I;Kim, C. K;Lee, B. S;Ha, T. K
  23. J. Comput. Chem v.10 Stewart, J. J. P
  24. J. Comput. Chem v.10 Stewart, J. J. P
  25. MOPAC 93 Manual(Revision Number 2) Stewart, J. J. P
  26. MOPAC 6.0 program, available from Quantum CHemistry Program Exchange (QCPE),No. 506
  27. J. Comput. Chem v.7 J. Baker
  28. Angew. Chem v.19 Muller, K
  29. J. Chem. Phys v.80 Bell, S;Crighton, J. S
  30. Adv. Phys. Org. Chem v.4 Bell, R. P
  31. Disscuss. Faraday Soc v.39 Eigen, M
  32. J. Am. Chem. Soc v.108 Madura, J. M;Jorgensen, W. L
  33. J. Mol. Struc. (Theochem) v.20 Ventura, O. N;Coitino, E. L;Irving, K;Iglesias, A
  34. Can. J. Chem v.69 Peeters, D;Leroy, G
  35. Int. J. Quantum Chem v.40 Ventura, O. N;Apostolova, E. S
  36. J. Am. Chem. Soc v.117 Wolfe, S;Kim, C. K;Yang, K;Weinberg, N;Shi, Z
  37. J. Am. Chem. Soc v.113 Cramer, C. J;Truhlar, D. G
  38. AMSOL 5.0 program available from Quantum Chemistry Program Exchange (QCPE), No. 606
  39. J. Chem. Soc. Perkin Trans. 2 v.799 Klamt, A;Schuurmann, G
  40. J. Comput. Chem v.13 Cramer, C. J;Truhlar, D. G
  41. J. Phys. Org. Chem v.10 Lee, I;Kim, C. K;Lee, B. S;Kim, C. K;Lee, H. W;Han, I. S
  42. J. Comput. Chem v.16 Liotard, D. A;Hawkins, G. D;Lynch, G. C;Cramer, C. J;Truhlar, D. G
  43. J. Am. Chem. Soc v.100 Benson, S. W
  44. J. Am. Chem. Soc v.114 Benson, S. W;Siebert, E. D
  45. ACS symposium Series 568 Structure and Reactivity in Aqueous Solution: Characterization of Chemical and Biological Systems Clementi, E;Corongiu, G;Cramer, C. J(Ed.);Truhlar, D. G(Ed.)